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FDA 510(k)

FS SERIES WHEELCHAIR

K-Number: K041814 · 2004-07-20

Decision Date2004-07-20
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FS SERIES WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Foshan Dongfang Medical Equipment Manufactory(Ltd). It received FDA 510(k) clearance on 2004-07-20 under 510(k) number K041814. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FS SERIES WHEELCHAIR?

FS SERIES WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2004-07-20. The listed applicant is Foshan Dongfang Medical Equipment Manufactory(Ltd). The 510(k) number is K041814.

When did FS SERIES WHEELCHAIR receive FDA 510(k) clearance?

FS SERIES WHEELCHAIR received FDA 510(k) clearance on 2004-07-20, under 510(k) number K041814.

Who is the listed applicant for FS SERIES WHEELCHAIR?

The FDA 510(k) record lists Foshan Dongfang Medical Equipment Manufactory(Ltd) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FS SERIES WHEELCHAIR?

The FDA product code for FS SERIES WHEELCHAIR is IOR.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: IOR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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